Associate Quality Control Analyst - Onsite

Title: Associate Quality Control Analyst - Onsite

Mandatory skills:

Quality Control, QC,
Microsoft Office, Excel, Word,
manufacturing, GMP,
environmental monitoring, subculturing, identification of organisms,
QC OOS Investigations, Quality Event reports, production, laboratory,
quality improvement, continuous improvement, lean, 5S,
performance testing, data specification, safety practices, hazards,
organizational, communication, problem solving, troubleshooting, decision making

Description:

Position Summary:
Seeking a detail-oriented and motivated Temporary Associate Quality Control Analyst (QC). This role will support the quality of our products. This position must be able to prioritize to ensure schedule and goals are met. Responsible for ensuring performance testing meets data specifications. Perform all duties using safety conscious practices. This is an excellent opportunity for individuals passionate about quality and continuous improvement within a manufacturing industry.

Primary Duties:
Test product lots as scheduled in an efficient manner per procedures and specifications.
Performs environmental monitoring, subculturing and identification of organisms.
Initiate Quality Event reports (QEs) for Finished Good testing and Environmental Monitoring Program.
Initiate QC OOS Investigations.
Supports continuous improvement processes in QC and replenishment of QC supplies using lean standards (5S).
Support QC and special projects that may arise in other departments as requested by management.
Promote a safe workplace by identifying potential hazards, wear appropriate PPE, and review safety procedures regularly and how to integrate them into daily activities.

Training and Education:
Bachelor s Degree
0-3 years of experience in quality control, or related field.
5+ years of experience accepted in lieu of degree and type.

Experience:
Requires a 4-year degree in biology or related field and 0-3 years of experience in quality control, or related field.
Strong attention to detail and organizational skills.
Requires strong computer skills including Microsoft Office Package (Excel, Word, etc.).
Must have a knowledge of GMP compliance.
Must be able to demonstrate flexibility in responding to unexpected demands. Must also be able to work in team environment, building effective working relationships.
Excellent written and verbal communication skills

Knowledge, Skills, and Abilities:
Makes decisions based on defined guidelines and procedures. Performs trouble shooting and applies problem solving skills to determine cause of problem areas.

Working Conditions and Physical Requirements:
Ability to remain in stationary position, often standing, for prolonged periods.
Ability to ascend/descend stairs, ladders, ramps, and the like.
Ability to wear PPE correctly most of the day.
Excellent personal hygiene and appropriate PPE is required in production and laboratory areas.
May operate in an environment with cool temperatures, low humidity, constant noise, or with occasional environmental odors.

Notes:
Monday - Friday Day Shift

VIVA USA is an equal opportunity employer and is committed to maintaining a professional working environment that is free from discrimination and unlawful harassment. The Management, contractors, and staff of VIVA USA shall respect others without regard to race, sex, religion, age, color, creed, national or ethnic origin, physical, mental or sensory disability, marital status, sexual orientation, or status as a Vietnam-era, recently separated veteran, Active war time or campaign badge veteran, Armed forces service medal veteran, or disabled veteran. Please contact us at for any complaints, comments and suggestions.

Contact Details :

VIVA USA INC.
3601 Algonquin Road, Suite 425
Rolling Meadows, IL 60008